Electrogel process for removing electrolytes and concentrating the same from an aqueous solution

ABSTRACT

An electrolytic continuous method for simultaneously removing electrolytes from aqueous solution and concentrating the electrolytes produced therefrom which comprises subjecting an aqueous electrolyte solution to contact with an inorganic oxide gel under the influence of an electrical field, allowing the electrolyte to be sorbed by the gel until a point of saturation is achieved, whereby the electrolyte is exuded from said gel and then recovering the resultant electrolyte exudate from said gel. Conveniently, the apparatus comprises at least one electrolyte concentrating unit comprising an inorganic oxide gel core encased within an open module having a bottom wall and a pair of parallel opposing sides and opposing end walls and whose opposing sides further comprise a cation-permeable membrane and an anionpermeable membrane, respectively, and a source of an applied electrical field.

United States Patent [1 1 Wallace 1 Feb. 27, 1973 [76] Inventor: Richard A. Wallace, 9707 Fourth Avenue, Brooklyn, N.Y. 11210 [22] Filed: March 27, 1970 [21] Appl. No.: 23,311

[52] US. Cl. ..204/l80 G, 204/180 R, 204/301,

204/180 P [51] Int. Cl. ..B0ld 13/02, B01k 5/00, C02b H82 [58] Field of Search ..204/180 G, 301, 299, 180 R [56] References Cited UNITED STATES PATENTS 1,235,064 7/1917 Schwerin ..204/1 80 R 1,546,908 7/ 1925 Lapenta ..204/180 R 1,603,298 /1926 Speed ..204/180 R 2,566,308 9/1951 Brener ..204/180 R 2,788,319 4/1957 Pearson ..204/180 R 3,255,100 6/1966 Raymond ..204/l G 3,533,933 10/1970 Strauch ..204/ G Primary Examiner-John H. Mack Assistant Examiner-A. C. Prescott Attorney-Charles J. Speciale [57] ABSTRACT An electrolytic continuous method for simultaneously removing electrolytes from aqueous solution and concentrating the electrolytes produced therefrom which comprises subjecting an aqueous electrolyte solution to contact with an inorganic oxide gel under the influence of an electrical field, allowing the electrolyte to be sorbed by the gel until a point of saturation is achieved, whereby the electrolyte is exuded from said gel and then recovering the resultant electrolyte exu-' date from said gel. Conveniently, the apparatus comprises at least one electrolyte concentrating unit comprising an inorganic oxide gel core encased within an open module having a bottom wall and a pair of parallel opposing sides and opposing end walls and whose opposing sides further comprise a cation-permeable membrane and an anion-permeable membrane, respectively, and a source of an applied electrical field.

28 Claims, 8 Drawing Figures DESALTED WATER OUT (EFFLUENT) PATENTH] FEB 2 71973 SHEET 10F 2 DESALTED WATER OUT (EFFLUENT) FIG. 2 3 BRINE EXUDATE 24 552 k-BRlNE FL f CL 1 I a Nq CONCENTRATION OF DESALTED WATER (EFFLUENT) EQUlV/LITER o INVENTOR. RICHARD A. WALLACE ATTORNEY QUANTITY OF ELECTRICAL CHARGE PASSED (FARADAYS) (EFFLUENT) CONCENTATION OF DESALTED VOL.OF OVERFLOW OF BRINE EXUDATE (ml) WATER EQUIV./LITER PAIEIIIEU SHEET 2 [IF 2 FIG. 5

E [U C 3 RUN I g 3 2 Q 2oo- I 3:

3; 2 an: 9% LLIO 2U IOO- 25g 1 ..1 LI- 0: LL] O QUANTITY OF ELECTRICAL CHARGE PASSED (FARADAYS) FIG. 7

FIG. 6

RUN I FIG. 8

QUANTITY OF ELECTRICAL CHARGE PASSED (FARADAYS) RUN II .050

QUANT. OF ELECTRICAL CHARGE PASSED (FARADAYS) INVENTOR.

RICHARD A. WALLACE ATTORNEY ELECTROGEL PROCESS FOR REMOVING ELECTROLYTES AND CONCENTRATING THE SAME FROM AN AQUEOUS SOLUTION BACKGROUND OF THE INVENTION 1. Field of the Invention:

This invention relates to an electrolytic method for removing electrolytes from aqueous solutions containing them and to concentrating the electrolytes produced thereby.

2. Description of the Prior Art:

Demineralization of water by electrodialysis and electrosorption and desorption processes is of course well known. Electrodialysis, the use of electrical potentials to trap concentrated brine between membranes composed of ion exchange materials is widely known. It is also known to be a complicated procedure and also a very uneconomical one. It involves the use of anion exchange resin membranes and cation exchange resin membranes, each of which will be permeable to ions bearing a given charge, but not to ions bearing the opposite charge. Thus membranes that are permeable to anions are marked with a positive charge, while those that are permeable only to cations are marked with a negative charge. However, not only are these membranes quite expensive, costing about $12.00 per square foot, but they are also subject to problems of scaling and fouling, so that they must be constantly, either cleaned or replaced. Desalination by electrosorption and desorption suffers from the same problems in that the base films coated with condensation-type ion exchange resins act in a manner similar to the cation exchange and anion exchange resin membranes described immediately above.

It would therefore be a tremendous advantage if an economical and uncomplicated process could be found for removing electrolytes from aqueous solutions containing the same.

SUMMARY OF THE INVENTION In accordance with the invention, there has now been discovered an electrolytic method for simultaneously substantially removing electrolytes from aqueous solutions containing the same, and concentrating the electrolytes produced thereby which comprises subjecting an aqueous solution containing the electrolytes to contact with an inorganic oxide gel under the influence of an electrical field, allowing the electrolyte to be sorbed by said gel until a point of saturation is achieved, whence the electrolyte is exuded by the gel, by a phenomenon known as syneresis, and then recovering the resultant electrolyte exudate as overflow from said gel.

The apparatus for simultaneously removing and concentrating electrolytes from an aqueous solution containing the same comprises at least one electrolyte concentrating unit which further comprises an inorganic oxide gel core encased within an open module having a bottom wall and a pair of parallel opposing sides and opposing end walls, said opposing sides further comprising a cation-permeable membrane and an anionpermeable membrane, respectively, and a source of an appliable electrical field.

While the apparatus and method broadly encompasses within its scope, the simultaneous removal and concentration of electrolytes from aqueous solutions containing the same, it has been found that this apparatus and method are particularly suitable, for example, for desalinating brine solution, such as in sea water and brackish waters, and concentrating the brine exudate produced therefrom, for removing excess citric acid from tart orange and grapefruit juice and concentrating the citric acid exudate, for removing and concentrating radioactive electrolytes from waste aqueous streams, and for removing excess sulfuric acid and other electrolytes, such as ferric salts, from acid mine drainage streams of low pH and high hardness, and simultaneously to concentrate the waste sulfuric acid effluent and other electrolytes to a point where it is readily disposable and still regenerate the original water for further usage. Brine desalination is of particular importance to areas where either fresh water is in short supply, or, where salt is the desired end product. The sweetening of citric juices is of course of particular importance to that industry whereby no added sugar is necessary. Removal of radioactive electrolytes is of considerable advantage today where pollution is a problem, and the removal of sulfuric acid and other electrolytes from mine drainage streams is equally important to present day pollution problems. Another area of importance is in the recovery of concentrated sulfites from spent pulping liquors in the paper industry and, it has been found that the present apparatus is quite useful in this application. The present apparatus and method are also particularly suitable for the removal and concentration of zinc salts from acidic aqueous electrolytes. This is of particular interest in the leather tanning industry.

BRIEF DESCRIPTION OF THE DRAWINGS The invention will be more fully understood with reference to the accompanying drawings in which:

FIG. 1 is a fragmented view in perspective showing a plurality of the invention gel modules interspersed between a source of an electrical field comprising a positive and negative electrode.

FIG. 2 is a side elevational view of one of the modules of the invention and as shown at a slight incline to the norm.

FIG. 3 is a sectional view taken along line 2-2 of FIG. 2 in the direction of the arrows.

FIGS. 4 to 8 are plots of results achieved in accordance with the method of the invention.

DESCRIPTION OF THE SPECIFIC EMBODIMENTS Referring now to the figures of the drawings, each invention module 10 comprises an elongated body having a bottom wall 12, a pair of parallel opposing end walls 14 and a pair of parallel opposing sides 16 and 18, respectively. Opposing side 16 further comprises a cation-permeable membrane which will be more fully described hereinbelow, and opposing side 18 further comprises an anion-permeable membrane which will be similarly described. The resulting module 10 is open at the top as at 20 and there is defined between the opposing sides 16 and 18 and opposing end walls 14, an elongated channel 22. Into this channel is placed an initially liquid inorganic oxide gel 24, whose composition will be described subsequently. Thus, a battery of these modules 10 can be placed in compartmented fashion within a frame 30 containing suitable elongated tracks 32 along the inside bottom 33 thereof into which each module is slidingly inserted. In turn, this battery of modules is interspersed between a source of an electrical field supplied by a graphite anode 34 and a stainless steel cathode 36. Each module may be constructed of any suitable rigid material, such as plastic, e.g. plexiglass, or the like. Preferably, for a reason that will become readily apparent, the modules, when in use, are inclined either longitudinally at a slope from the normal, or transversely, at a slope from the normal.

The inorganic oxide gel core is formed of a suitable polymerizable compound. The requirements of a suitable inorganic oxide gel coming within the scope of the invention have been found to be as follows:

1. The gel must be non-elastic and essentially nonswelling.

2. The gel titania, have high electrical conductivity and salt diffusivity in the presence of electrolytic solutions.

3. The gel must readily undergo syneresis under its own gel we.ght.

4. The gel must substantially undergo the process of imbibition and exudation of electrolytic solutions over periods of months without attendant gel breakdown.

5. The gel must be hard and stable over several months in electrolytic solutions.

6. The gel must be compatible with the ion permeable membranes.

It has been found that such gels fall within elements in the Periodic Table coming from the Groups III-A, IV-A, IV-B, V-B, VI-B, VII-B, VIII and rare earths. As illustrative of such inorganic oxide gels may be listed: silicic acid; vanadium pentoxide; manganese dioxide; cerric hydr-oxide; zirconium hydroxide, molybdate, borate; ferric phosphate, arsenate, borate; chromium phosphate, arsenate, borate; and stannic hydroxide, borate, and tungstate.

The inorganic oxide gel employed may also consist of a plural gel comprising a predominant amount of silica with one or more metals or oxides thereof selected from Groups I-B, II, III, IV, V, VI, VII and VIII of the Periodic Table.

Particular preference may be given to plural gels of silica with metal oxides of Groups II-A, III and IV-A, especially wherein the metal oxide is magnesia, rare earth, titania, beryllia,.thoria, or combinations thereof.

The preparation of plural gels is well known and generally involves either separate precipitation or coprecipitation techniques in which a suitable solid of the metal oxide is added to an alkali metal silicate, and an acid or base, as required, is added to precipitate the corresponding oxide. The silica content of the siliceous gel matrix contemplated herein is generally in the range of 55 to 100 Weight percent with the metal oxide content ranging from to 45 weight percent. In a preferred mode of operation, silica gel is employed as the core material for the module. Silica gel is a solid resulting from the reaction of sulfuric acid and sodium silicate as may be represented by the following formula:

Na SiO xH O H 80 SiO (x+1) H O P182504 This reaction mixture is poured into the elongated channel of the module as defined hereinabove and solidification of the polymer is brought about when the polysilicate acid is formed from the reaction. The rate at which polymerization takes place depends on the proportion of sulfuric acid to sodium silicate and the concentrations of these reactants. This is well known to the art. The greater the percentage of sodium silicate in the reaction mixture and more concentrated the acid and silicate are, the faster the gel will set and the more solid it will become. In typical gel formation 40 ml. of 6 molar silicate solution when mixed with 15 ml. of 10 molar sulfuric acid, which mixture is allowed to stand for about 10 minutes when poured into the gel compartment and allowed to polymerize, will yield a hard gel solid. Over-night hardening of the gel is highly desirable. Before use, the hardened gel is leached of excess acid electrically for about 12 hours by reversing the field polarities so that the electrolytes in the gel structure are removed from the gel and discharged into the surrounding solution. This will become more readi- 1y apparent subsequently.

The operation of the invention apparatus will now be described in greater detail. While it is to be understood that the invention apparatus and method are applicable in removing and concentrating any electrolyte from aqueous solutions, for ease of description, the method will be described in terms of desalinating a brine solution and concentration of the brine produced therefrom.

As mentioned, polymerized silica gel is sandwiched between a cation-permeable and anion-permeable membrane. Brine solution to be desalted flows on both sides of the membrane-gel module. Application of an electric field causes the ions to move towards the electrodes of opposite sign. Thus Na ions enter from the left side through the cation-permeable layer and into the gel. Since the anion-permeable membrane allows only negative ions to pass through, the passage of Na ions out of the gel is prevented. Similarly Clions are transferred from right to left into the gel compartment. In this way, the feed solution is depleted of NaCl while the gel salt concentration builds up in the gel.

Together with the transport of ions, a concomitant phenomenon of electro osmosis occurs. The ions drag along water molecules into the gel. In addition, osmosis causes extra flow of water in the same direction. The gel can maintain a high percentage of concentrated salt solution. However, once its capacity is exceeded, it rejects the solution. Since the gel is bounded on both sides by the membranes, the flow of solution occurs upwards to the open face of the gel module at the top. At steady state conditions, the overflow rate becomes constant and equal to the net solution flow. Also, the amount of salt in the overflow will be equal to the amount of salt removed from the feed solution which in turn is related to the current flowing through the system.

As illustrated in FIG. 1, an electrogel demineralizer is composed of many gel modules arranged between a pair of electrodes in a manner that allows the brine solution to be demineralized, i.e. desalted, to flow between the parallel surfaces of the gel modules. When voltage is applied to the electrodes, cations go from the solution through the cation-permeable layers into the inner gel layer but are blocked from going further by the anion-permeable layer. Simultaneously, the anions are transported in the opposite direction through the anion-permeable surface into the gel core, but are blocked in turn from going through the modules by the cation-permeable layer. Thus, electrolyte (NaCl) is trapped inside the gel and the external solution is desalted as it flows through the spaces of the gel module. As this operation continues, the solution in the gel becomes concentrated with electrolyte. The gel then undergoes appreciable shrinkage in volume with a simultaneous exudation of concentrated brine. The gel phenomenon is called syneresis.

Silicic acid gel has an ability to distribute salt between itself and the external salt solution, the rate of salt concentration varying greatly with different ions. The diffusivity and conductivity in the silica acid gel is high so that, as a result, there is negligible electrical resistance and polarization at the gel interfaces.

Using this apparatus and method as high as 20 times desalination over the brine feed can be achieved. The volume of gel brine overflow is linear with the quantity of electrical energy (Faradays) used, except initially during the start of each run. It has been found that the gel, e.g. silicic acid, vanadium pentoxide, etc. maintains very high levels of salt up to about 4.5 N sodium chloride and 3.5 N potassium chloride.

The cation-permeable and anion-permeable membranes may be any commercially available membrane, some of which will be described in the examples immediately below. Alternatively, instead of one of the commercially available anion-permeable membranes, a neutral or slightly or moderately anionic anion-permeable membrane film, such as cellulose or loosely structured films of moderate anionic properties, may be employed. These latter membranes are characterized by slightly lower salt diffusion rates and electrical conductivities relative to conventional anion exchange membranes. Thus, if it is the purpose of the operation to concentrate brine, I then the commercially available anion-exchange membrane will be used, whereas, if it is desirous to desalinate brackish solution, then the neutral or moderately anionic permeable membrane will be employed, so that much higher current densities can be obtained. A typical ion-permeable membrane employed in the invention will have the following specifications:

1. Electrical resistance in 0.01 I l NaCl less than ohm-cm 2. Anion-transference number :'t' as calculated from concentration potential measurements between 0.010 and 0.005lj NaCl: 0.65 to 0.85.

3. Cation-transference number: 71, as calculated from concentration potential measurements between 0.010 and 0.0051j NaCl 0.75 to 0.98.

4. Salt diffusion measured between 0.1111 NaCl and distilled water: 10" to 10" gram equivalent/cm -hr.

5. Acid diffusion measuiied between 0.002l lH SO and distilled water: 10' to 10' gram equivalent/cmhr.

6. Burst strength by standard Mullen Burst tester: greater than 30 psi.

7. Water-permeability: less than 10' mllsec-cm -psi.

8. Electroosmotic water transport: less than 13 moles per Faraday.

Thus, electrogel desalination, in accordance with the invention, is a continuous process in which ions acting under the force of applied electrical field are transported and concentrated in gel modules. At the same time, the gel rejects this concentrated salt as brine overflow at the top of the gel. It will now be readily apparent why it is highly desirable to tilt the gel module, i.e. at a slope deviated from the normal, either longitudinally or transversely, and that is to allow for greater ease of brine overflow and concentration. Any brine overflow will flow down the slope to its collection chamber.

The advantages of the invention electrogel desalinator with respect to conventional electrolytic processes are manifold. Among these may be included:

1. More economical and simpler stack construction than related electrodialysis and electrosorption desalting processes.

2. Produces a high concentration of brine (ratio of brine concentration to feed concentration may range from about 6:1 to 20:1

3. Eliminates one process stream thereby lowering storage, pumping and piping requirements.

4. Treats feeds that are high in CaSO, with little difficulty.

5. Process is continuous and requires no regeneration.

6. Higher gel-membrane area utilization.

This invention will be further illustrated in conjunction with the following specific experimental runs which will serve as Examples of the invention. All of the ion-permeable membranes employed hereinbelow will be understood to meet all the required specifications as set forth earlier, whether mentioned specifically, or not. While the present invention has been described in terms of preferably a continuous method of operation for simultaneously removing and concentrating electrolytes from aqueous solutions containing the same, it is to be understood that the method may also be practiced in a batch-wise operation.

RUN l (CONCENTRATED FEED) The results of this run are presented in FIGS. 4 to 6. The effluent concentration, brine-exudate gel overflow volume, and overflow concentration are all plotted against the quantity of electrical energy passed through the gel desalination set-up. A silicic acid gel module was used. The cation-permeable membrane was an Ionics Nepton Cr-6l cation-exchange heterogeneous membrane consisting of sulfonated vinyl-divinyl benzene copolymer with Dynel fabric backing. This membrane has an ion-exchange capacity of 2.7 meg/gram and a water transport of l 1 moles water per Faraday. The anion-permeable membrane was an Ionics Nepton AR-IIIA anion-exchange heterogeneous membrane consisting of quaternary ammonium basic groups on a vinyl-divinyl benzene base with dynel backing. This membrane has an ion-exchange capacity of 1.8 meg/gram and a water transport of 6 moles water per Faraday.

Current Efficiency 1 Brine-exudate overflow N =2 N (final cone.) V0 =370 cc.

Feed Gel Eflilucut Nr=0.38 N desalinator N =0.20 N Y! 10,000 cc. VF, =9500 cc.

1 1 t Efilucnt test samples N ET =0.24 N (average) V ET cc.

Q I X 1 12,840 coulombs Final Desalination Ratio N lN l12,840/96,500 2N/0.2N

= 1.17 Faradays 5 The concentration ratio is obtained from the brine For each Farada assed, theoreticall one e uivalent y p y q overflow con-centration and the feed concentration:

of salt goes into the gel compartment and another equivalent of salt goes into the electrode com-part- Final Concentration Ratio: No/Nl ment. Hence, 10

Theoretical Salt Removed 2 X Q 5 3 =2 SeeFIGS.4,5and6- 234 equivalents Again, the effluent concentration, brine-exudate gel overflow volume and concentration are plotted against the quantity of electrical energy in Faradays passed Now the actual salt removed 18 the difference in the salt through the electrogel System.

in the feed and the salt in the effluent.

20 RUN II DILUTE SALT EED Initial Salt in Feed 0.38 X 10 3.8 equivalent F The .results of Run II are shown in FIGS. 7 and 8. The Final Salt Effluent: equivalent Ionics Nepton CR-6l cation-exchange membrane and the Ionics Nepton AR-IIIA anion-exchange membrane were used as the outer films in the silicic acid gel Overall Current Efficiency (Actual Salt Removed X module- 100/Theoretical Salt Removed) Actual Salt Removed 2.10 equivalent Brine-exudate overflow 3O Nuflfi N Na Cl 90% V,,fl8 cc.

Current Density lieed water G L 3 N Nucl NE=0.01u N NnCl Initial Current Density, MA 100 ma/5 cm 20 VE=4,850 cc.

ma/cm Final Current Density, I,/A 80 ma/S cm 16 ma/cm Q I X 0= 21,720 coulombs Cell Resistance 21 ,720/96,500 0.225 Faradays 40 Initial Resistance, R, E,/I, (9.6 volts/100 X 10' Overall Current Efficiency Actual Salt amp) Removed/Theoretical Salt Removed Final Resistance, R E;/I,= (9.8 volts/8O X 10' amp) Operative Current Density 123 0 For Run II= l6 (mA/cm Electro Osmotic and Osmotic Flow Rate Desalination Ratios From the straight line portion of the brine-exudate Fmal Desalmauon Ramos N/NE overflow volume vs. Quantity of Faradays plot in FIG. 1,6 N0 O1O N 5, at

160 Q 1 Faraday Final Salt Concentration N /N,

V,,=314 cc. 1.6 N/0.082

W=314cc/1Faraday=314cc/F 19.5

= 314/1 17 4 moles f H Q/F d Thus, feed water was concentrated 19.5 times.

See FIGS. 7 and 8. Desalination Ratio Interpretation of FIGS. 4-8

. The desalination ratio is obtained from the overall FIGS. 4 (Run I)and 7 (Run 11) giving the effluent salt Brine con-centration and the effluent product concenconcentration versus quantity of electrical energy Q tratlon: (Faradays) passed through the system were both apgals $2921 zeaspnah s.

proximately linear. This means the overall current efficiency of the electrogel process was fairly constant with feed concentration. The calculated efficiencies were 90 percent and 85 percent for the concentrated 0.38 N NaCl and dilute 0.082 N NaCl feed respectively. These coulombic efficiencies were about the same as that of bench-scale electrodialysis. As expected, the efficiency for the dilute salt feed solution was lower than that of concentrated feed because of somewhat higher electroosmosis and osmosis.

In FIGS. (Run I) and 8 (Run II), the volume of brine-exudate overflow was linear with the quantity of electrical energy Q (Faradays) passed through the system, except during the unsteady-state period at the start of each run. For the concentrated feed in Run I, a water flow rate of 17.4 moles of R 0 per Faraday is obtained at an average current density of 18 malcm At this level of current density, the electroosmotic flow These two runs clearly show that the gel is able to maintain and exude a high concentration of brine product. As FIG. 6 (Run 1) shows, after an initial unsteady-state period, the brine-exudate overflow concentration becomes constant at 2.0 N NaCl for the concentrated 0.38 N NaCl feed of Run I and 1.6 N NaCl for the dilute 0.082 N NaCl feed of Run II. Hence,

{decreasing the feed salt concentration by 78 percent,

only lowers the brine-exudate gel overflow concentrat New? Per s!"- The prior art electrodialysis method must operate at low current densities (below 20 mA/cm especially when treating high-hardness brackish waters or pH- sensitive solutions because of excessive polarization and scaling of the troublesome anion-permeable membrane. I

The present electrogel method, however, can treat these brackish waters at very high current densities (above 40 mA/cm), providing an anion-permeable film or a membrane with slight or moderate anionic properties is used. The electrogel process has the unique advantage of producing a highly concentrated electrolyte or brine product simultaneously.

RUN III (SILICIC ACID GEL) A clear and very hard gel was made by reacting one part of concentrated sulfuric acid (H 50 specific gravity 1.8 to 4 parts of sodium silicate (Na SiO This viscous mixture solidified in about minutes after being poured in the gel module.

Brine-exudate Feed Efliuent Nr=0.20 N NE=0.025 V=10,000 cc. VE=9,850 cc.

Overall Current Efficiency 89% Operative Current Density for Run III 18 mA/cm 15 Desalination Ratios Final Desalination Ratio N /N l.9N/0.025N 76 Final Salt Concentration N,,/N,= l .9N/0.20N

RUN IV (MIXED FEED NaCl 0.10 N CaSO 0.05

N SOLUTION A 114 moles H 50, sio, silicic gel was used along with Asahi Glass Companys Selemion CSI-I strongly acid membrane and Selemion ASG basic membrane.

Gel overflow Vn=150 cc. No=l.40 N NaCl =0.008N CaSOA Feed Effluent N1=0.10 N NaCl NE=0.030 N NaCl =0.05 N (32:50.; =0.0i0 N CaSO4 4O V=10,000 cc. V =9,800 cc.

The Asahi Glass Companys Selemion CSI-I strongly acidic membrane is selective only for univalent cations.

This membrane is a laminate of a regular cationexchange membrane with a crosslinked phenolic coating pointed on the membrane surface. This tight coating allows monovalent cations through but stops 5o divalent cations such as calcium and magnesium ions.

The Asahi Glass Company's Selemion ASG strongly basic membrane is selective only for univalent anions. Also, this membrane is a laminate of a regular anionexchange membrane with a crosslinked aminated coating pointed on the membrane surface. This tight coating allows monovalent anions through but stops divalent anions such as sulfate anions.

Overall Current Efficiency 82% Operative current density for Run IV 12 mA/cm Desalination Ratios Final Desalination Ratio N /N Final Salt (NaCl in the presence of CaSO in feed) Concentration N,,/N,

using univalent-permeable Selemion membranes that block transport of divalent calcium and sulfate ions.

RUN V (GEL MODULE USING SLIGHTLY ANION- PERMEABLE [LOOSELY STRUCTURAL] MEMBRANE Silicic Gel: 1:4 molar ratio of Membranes Used: Ionics Nepton CR-6l cationexchange membrane and slightly anionic or modified neutral lonac Chemical Company's membrane (used now in the transport-depletion electrodialytic process). The membrane used had the properties: 75 percent anion permselectivity, 20 percent gel water content, minimum crosslinking, and high salt-diffusion rates of 1.4 X 10 (gram equivalent) cm hr.

N1=3.0 N NaCl V =l0,000 cc.

Overall Current Efficiency 55% Operative Current Density for Run V 55(mA/cm Desalination Ratios Final Desalination Ratio N /N 3.0/0.46 6.5

Final Salt Concentration N,,/N,= 3.0/O.60 5.0

RUN VI This Run was substantially similar to Run II with the exception that the anion-exchange membrane was replaced by a nonselective plastic membrane film and the silicic gel was a 1:4 (H 80 Ha SiO molar ratio.

NE=0.09 N NaCl V =l0,000 cc.

VE=9,650 cc.

Overall Current Efficiency 48% Operative Current Density for Run VI 55-60(mA/cm Desalination Ratios Final Desalination Ratio N,,/N l .0/0.09

Final Salt Concentration N /N,= 1.0/0.2

RUN VII Overall Current Efficiency 80% Operative Current Density for Run Vll 15(mA/cm Desalination Ratios Final Desalination Ratio N,,/ N E Final Salt Concentration N /N,

RUN VIII This Run was substantially similar to that of Run VI with the exception that the gel was ferric arsenate gel.

The outer layers of the gel module are Ionics membranes described in previous runs.

The sol of ferric arsenate was obtained by adding potassium arsenate solution to a ferric chloride solution. Five mililiters of the sol were mixed with 0.5 Norma] potassium sulfate to form a stable gel in the module. The sol content was 31 grams of ferric arsenate per liter.

Gel

Overall Current Efficiency 80% Desalination Ratios Final Desalination Ratio N /N 1.3/0.03 43 Final, Salt Concentration N,,/N,= 1 .3/0.1o 13 RUN IX This Run was substantially similar to that of Run V1 with the exception that the gel was zirconium borate gel.

Gel Preparation The zirconium borate sol was prepared by mixing a solution of zirconiumnitrate and a concentrate borate solution. The zirconium borate content was about 15 grams per liter. The gel was formed on adding a 0.4 Normal solution of potassium sulfate. The gel readily synerized and was quite stable in potassium sulfate salt solution.

. Gel

This Run was substantially similar to that of Run V1 with the exception that the gel was ferric phosphate gel. Ferric phosphate gel the sol of ferric phosphate was prepared by adding potassium phosphate to 3 N ferric chloride solution in slight excess and electrodialyzing the sol mixture for 24 hours. The ferric phosphate sol content was 54 grams per liter and was coagulated by 0.5 Normal potassium sulfate solution. The ferric phosphate gel readily synerized in the presence of potassium sulfate solutions. -M my Gel .14 Overall Current Efficiency Operative Current Density for Run X 18(mA/cm) Desalination Ratios Final Desalination Ratio N IN 1.0/0. 1 2 8.5

Final Salt Concentration N /N,= l .0/0.20

Sweetening of Citrus Juices (Deacidification) A problem in the citrus industry exists. Each year a large portion of the orange and grapefruit crop yields a juice that is too tart in flavor for full customer acceptance. This tartness can be reduced satisfactorily by the removal of excess citric acid. Currently, this problem is handled in one of two ways: by blending the tart juice with sweeter juice that has been produced at a different time in the growing season; or, by the addition of sugar to the tart juice. Both of these alternatives create problems of their own. In the first case, there are problems of juice storage and juice availability. In the second case, the addition of sugar creates a departure l from the pure, unadulterated citrus juice. A third alternative method was proposed for the reduction of acid from fruit juices by an ion-exchange resin column. This method applied the electrodialysis process in the reduction or removal of excess citric acid from tart fruit juices. It comprised an all-anion membrane electrodialysis stack. In this scheme, citrate ions in the juice move through the anion membranes toward the anode into alternating potassium hydroxide cells. Equivalent quantities of hydroxyl ions move from the potassium hydroxide cells into the juice cells to neutralize the hydrogen ions. The net result is the removal of excess citric acid.

This invention provides a much simpler (in mechani- Dilute potassium hydroxide solutions were used only in the anolyte and catholyte electrode compartments of this electrogel deacidifier. In the prior art, all anionmembrane electrodialysis process, however, dilute potassium hydroxide is used in every alternate cell compartment in order to neutralize the hydrogen ions.

Deacidification of Citrus Juice By Electrogel Process The net reaction in the juice compartments is the removal of citric acid as a concentrated citric acidcitrate solution of gel exudate. The degree of acid removal was controlled by regulating the applied voltage or current, and the flow rate of the juice feed through the electrogel system.

.15, RUN XI I Exudate concentrated citric acid-l- K citrate solution Electrogel deacidifier (silicic gel mod Efliuent sweet (deacidified) 1185) i grapefruit juice Feed tart grapefruit juice sealants Dat;

= 6% total citric acid and potassium citrate content solution Exudate RUN XII Exudate concentrated citric aeid+ K citrate solution Efliuent sweet orange juice concentrate Electrogcl deacidifier (silicic gel modules) Feed concentrated tart orange juice Expe firnental Data Feed (concentrate orange juice) was clarified (suspended solids removed by centrifugation):

Feed Temperature lF. Feed Acidity 1.1% Effluent Acidity 0.4% Cell Velocity 0.10

FT/sec Applied Voltage 80 volts Current Density 10 ma/cm Current Efficiency 59% total citric acid and potassium citrate solution Exudate These two runs illustrate the successful application of the electrolgel method in removing excess citric acid and concentrating same from tart orange and grapefruit juices. Throughout our citrus deacidification runs, there was encountered a steady increase in the electrical resistance of the electrogel deacidifier system. This was caused for the most part by colloidal accumulations at the membrane surfaces. This problem was solved by means of periodic current reversal.

New frequent current reversal is urged as a means of operating this process with a minimal increase in cell resistance. Also, it was observed that a somewhat higher operating temperature (above room temperature) around 100F. gave good current efficiencies'of around 60%. Current densities in excess of 14 ma/cm caused degradation in the citrus juice itself.

In Runs XI and XII, the inorganic gel core was silicic acid gel and the cation-permeable membrane was commercially available AMF Co. C-60 membrane, while the anionpermeable membrane was ordinary cellulose film.

RUN XIII (REMOVAL AND CONCENTRATION OF ELECTROLYTES FROM ACID MINE DRAINAGE) Stream pollution resulting from mining operations is a serious problem in the Unites States and the world. Annually, approximately 500 billion gallons of mine drainage contain 5 to million tons of acid pollute over 10,000 miles of surface streams and more than 15 ,000 acres of impounded waters.

The basic problem stems from the formation of S111- furic acid from ferrous sulfide oxidation in waters emanating from both active and abandoned coal mines. The pollution is characterized by low pH, high hardness, and large amounts of ferric salt. The presence of these pollutants renders streams especially deleterious to aquatic life, both animal and plant; corrosive to metallic structures which come into contact; and unattractive from an esthetic viewpoint.

Presently, the chief method of acid mine pollution abatement is neutralization of the water wit lime or soda ash and subsequent oxidation of the ferrous to ferric iron followed by flocculation and removal of hydrous oxides of iron, manganese and aluminum.

Our experimental determinations demonstrated that typical acid mine drainage feed samples were desalted and deacidified directly by out electrogel process. The electrogel method continuously produced an overflow acidic concentrate stream of low pH and high salt content.

Typical Experimental Run Raw Acid Mine Drainage Stream Composition:

Raw Feed: Acid (H,SO level pH 3.0 Manganese and Aluminum sulfates 800 ppm. Iron (ferrous) sulfate ppm.

Acid \vastc Concentrate jas overflow (plI=i.'.l)

(lllmiv acid mine D H d d ra na cstream csa c an g u ii' l c n containing iron can 1 0 (lcacidilcd cl'llucnt salts (pH=3.9) (pI =4.4)

Cell Operating Data Cell Velocity Feed Current Density Current Efficiency 0.06 -I.5 FT/sec i0 -25 Ina/cm 42 48% Concentrated acid waste composition (pH 1.9) comprised sulfuric acid and sulfates of manganesium, aluminum and iron.

Composition of Effluent desalted stream was pH level Iron Sulfate 60 ppm Manganesium and aluminum sulfate 200 ppm Other monovalent salts I50 ppm Another typical run consisted of the treatment of a dilute solution of synthetic acid mine drainage, containing less than ppm iron salts by our electrogel method. An eleven-fold reduction in percent hardness and an increase in pH levels from 3.2 to 4.2 resulted when this synthetic acid mine water comprising 5,000 ppm of total calcium, magnesium and manganesium sulfates to which was added concentrated sulfuric acid to pH level of 3.2 was treated by our electrogel cell system operating at a -20 ma/cm current density and a feed flow rate of 0.] FT/sec.

In this run, our electrogel cell comprised of a cationpermeable membrane of 0.92 cation-transference number and an electroosmotic water transport between 4.0 and 9.0 moles per Faraday; an anion-permeable membrane of 0.75 anion-transference number and an electroosmotic water transport between 4 and 7.0 moles per Faraday. The inner core comprising silicic oxide gel was prepared from a 1:3 molar ratio of H 80, to Na SiO Our data showed that our electrogel process removed sulfuric acid, manganese, aluminum, calcium and magnesium salts, and simultaneously concentrated the same into a small volume for disposal. The efficiency of this method depended on the concentration of iron salts which acted as a foulant to our ion-permeable membranes. We found that these iron salts were also removed when we used more porous, less selective ionpermeable membranes in our electrogel method.

RUN XIV (RECOVERY OF CONCENTRATED SULFITES FROM SPEND PULPING LIQUORS BY ELECTROGEL DEMINERALIZATION) Technical management in pulp mills are very concerned with recovery of pulping inorganic chemicals (basic sulfites) in their pulping process. We have found that when the raw spent sulfite pulping liquors were processed in our Electrogel Demineralizer, we recovered large amounts of sodium, ammonium and magnesium sulfites as a highly concentrated solution. This concentrated sulfite solution may be re-used in the pulp digesters or recovered as valuable useful chemicals.

In comparing the currently-used electrodialysis cell plate and frame design, as described in US. Pat. No. 3,136,710; and Canadian Pat. No. 677,654, our electrogel concentration process produced a much higher sulfite concentrate with a simpler, single-pass cell arrangement instead of the more expensive plate and frame construction.

Saturated sulfite-rich overflow stream containing small amounts of sodium loi'mato and acetate lllnt-k spvnl.

h'ullito pulping liquor loud lrignin products llomlcollulnsv lignin sullonatos Elvctroucl Dvlnilu'mlizm' 3. The inner gel core was silicic acid gel prepared from H Na siO molar ratio of 1:3.

Test Runs Feed Treated: Raw Acid Sulfite Spend Pulping Liquor Feed volume 8 gallons Feed temperature 65C.

Feed pH 2.7

Cell velocity 0.2 FT/sec Applied average cell voltage volts Average current density 125 ma/cm Current efficiency 68% D.C. energy consumption 0.20 KW-hr/gal|on Percent full sulfite recovery (for reuse) collected as highly concentrated Mg, Na and NH, basic sulfites solution from sulfite-rich gel overflow stream Feed Treated: Raw Neutral Sulfite Spent Pulping Liquor Feed volume 6 gallons Feed temperature 50C. Feed pH range 6.5-8.0 Cell velocity 0.2 FT/sec Applied average cell voltage volts Average current density 120 ma/cm Current efficiency 65% D. C. energy consumption 0.22 KW-hr/gallon Percent full sulfite recovery (for reuse) collected as highly concentrated Mg, Na and NH basic sulfites solution from sulfite-rich overflow stream RUN XV (REMOVAL AND CONCENTRATION OF ZINC SALTS FROM ACIDIC AQUEOUS ELECTROLYTES) We prepared a number of acidic zinc solution comprising 3.0 percent (by weight) of ZnCL to which was added concentrated HCl to yield solutions at various acid levels within the pH range 2.5-6.0.

We treated a number of these zinc salt solutions by our electrogel method, and we measured the zinc chloride depletion in the desalted effluent and the concentration of zinc chloride in the overflow concentrate stream.

A cation-permeable membrane having a cationtransference number higher than 0.90 and an electroosmotic water transport of less than 7.0 moles per Faraday; and an anion-permeable membrane having an anion-transference number higher than 0.85 and an electroosmotic water transport of less than 5.0 moles per Faraday, were employed. The inner gel cores each comprised silicic oxide, individually prepared from a series of 1:1, 1:2 and 1:3 molar ratios of H 80 Na SiO A Typical Experimental Run Feed: gallons of 3.0% ZnCl solution, pH 4.0

Overflow concentrate stream: 14.0% ZnCl solution,

Effluent desalted stream: 0.9% ZnCl solution, pH

Flow Rate: 0.1-0.3 gallons per minute Temperature: 25C.

Current Density: 12-20 ma/cm Applied Cell Voltage: 95 volts RUN XVI (REMOVAL AND CONCENTRATION OF ELECTROLYTES FROM AQUEOUS RADIOACTIVE FlSSlON PRODUCTS BY THE ELECTROGEL PROCESS) Our Electrogel Process meets two special requirements in treating waters contaminated with radioactivity: first, the radioactive water is desalted to remove most of the radioactivity, and second, the salt is concentrated into a small volume of solution as overflow effluent to reduce the cost of final disposal.

A. Removal And Concentration Of Radioactive Strontium Salts Radioactive Strontium is one of the most biologically hazardous elements of the fission products because of its high retention in the body, and its concentration in the bone. The maximum permissible level for strontium 90 in water is 8 X microcuries/ml.

Radioactive tap water [pH 4.5] containing 500 ppm hardness (Na, Mg and Ca nitrates) and a level of strontium 90 nitrate of 1.0 X 10 microcuries/ml is used as the feed. Low flow rates of 0.05-0.40 gallons per minute are used in our method.

The membranes are: a cation-permeable membrane having a cation-transference number higher than 0.92 and an electroosmotic water transport of less than 7.0 moles per Faraday, and an anion-permeable membrane having an anion-transference number higher than 0.86 and an electroosmotic water transport of less than 5.0 moles per Faraday. The inner gel cores individually consist of silicic oxide, each preparable from a series of 1:1, 1:2 and 1:3 molar ratios of H 50 Na SiO A constant decontamination factor of is attainable by our method. The effluent desalted waste stream has a radioactive level below 0.67 X 10*" microcuries/ml. A moderate current density of 5-15 ma/cm is used.

B. Removal And Concentration Of Radioactive Cesium Salts The maximum permissible radioactive level for Cesium 137 in water is 1.5 X 10 microcuries/ml. Radioactive tap water (pH 5.0) containing 150 ppm hardness in calcium salts and 400 ppm sodium and potassium chlorides and a level of Cesium-1 37 of 8.0 X 10' microcuries/ml is decontaminated and desalted in out method. Low flow rates of 0.05-0.40 gallons per minute are used.

The membranes are: a cation-permeable membrane having a cation-transference number higher than 0.92 and an electroosmotic water transport of less than 16.5 moles per Faraday; and an anion-permeable membrane having an anion-transference number higher than 0.86 and an electroosmotic water transport of less than 5.0

moles per Faraday. The inner gel core consists of silicic oxide, preparable from 1:2 molar ratio of H Nazsiog.

A continuous decontamination factor of 20 is maintainable by our method. The effluent desalted waste stream has a radioactive level below 4.0 X 10' microcuries/ml. A moderate current density 5-15 ma/cm is used.

What is claimed is:

l. A continuous method for simultaneously removing and concentrating electrolytes from aqueous solutions containing the same which comprises subjecting an aqueous electrolyte solution to contact with an essentially non-elastic inorganic oxide gel maintained between a cation-permeable membrane and an anionpermeable membrane under the influence of an applied electrical field, allowing the electrolyte to be sorbed by said gel until saturation of said electrolyte occurs in said gel, whereby said electrolyte is resultingly exuded by said gel, and thence recovering the resultant electrolyte exudate as overflow from said gel.

2. A method according to claim 1 wherein said inorganic oxide gel is formed of the oxides of a metal selected from the group consisting of Groups Ill-A, lV-A, lV-B, V-B, Vl-B, Vll-B, Vlll are rare earths of the Periodic Table.

3. A method according to claim 1 wherein said inorganic oxide gel comprises a plural gel comprising a predominant amount of silica combined with at least one oxide of a metal selected from the group consisting of Groups l-B, 11, 111, IV, V, VI, VII and VIII of the Periodic Table.

4. A method according to claim 2 wherein said inorganic oxide gel is formed of silica.

5. A method according to claim 2 wherein said inorganic oxide gel is formed of vanadium pentoxide.

6. A method according to claim 2 wherein said inorganic oxide gel is formed of manganese dioxide.

7. A method according to claim 2 wherein said inorganic oxide gel is formed of cerric hydroxide.

8. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium hydroxide.

9. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium molybdate.

10. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium borate.

l 1. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric phosphate.

12. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric arsenate.

13. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric borate.

14. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium phosphate.

15. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium arsenate.

16. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium borate.

17. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic hydroxide.

18. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic borate.

19. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic tungstate.

20. A method according to claim 1 wherein said electrolyte is sodium chloride.

21. A method according to claim 1 wherein said electrolyte is citric acid.

22. A method according to claim 1 wherein said electrolyte is sulfuric acid.

23. A method according to claim 1 wherein said electrolyte is iron sulfate.

24. A method according to claim 1 wherein said electrolyte is zinc chloride.

25. A method according to claim 1 wherein said electrolyte is strontium nitrate.

26. A method according to claim 1 wherein said electrolyte is cesium 137 chloride.

27. A method according to claim 1 wherein said electrolyte is a member selected from the group consisting of sodium, ammonium and magnesium sulfites.

28. A method for simultaneously removing and concentrating electrolytes from aqueous solutions containing the same which comprises subjecting an aqueous electrolyte solution to contact with an unit comprising an inorganic oxide gel core encased between two membranes under the influence of an applied electrical field, allowing the electrolyte to be sorbed by said gel until saturation of said electrolyte occurs in said gel, whereby said electrolyte is resultingly exuded by said gel, and thence recovering the resultant electrolyte exudate as overflow from said gel. 

2. A method according to claim 1 wherein said inorganic oxide gel is formed of the oxides of a metal selected from the group consisting of Groups III-A, IV-A, IV-B, V-B, VI-B, VII-B, VIII are rare earths of the Periodic Table.
 3. A method according to claim 1 wherein said inorganic oxide gel comprises a plural gel comprising a predominant amount of silica combined with at least one oxide of a metal selected from the group consisting of Groups I-B, II, III, IV, V, VI, VII and VIII of the Periodic Table.
 4. A method according to claim 2 wherein said inorganic oxide gel is formed of silica.
 5. A method according to claim 2 wherein said inorganic oxide gel is formed of vanadium pentoxide.
 6. A method according to claim 2 wherein said inorganic oxide gel is formed of manganese dioxide.
 7. A method according to claim 2 wherein said inorganic oxide gel is formed of cerric hydroxide.
 8. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium hydroxide.
 9. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium molybdate.
 10. A method according to claim 2 wherein said inorganic oxide gel is formed of zirconium borate.
 11. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric phosphate.
 12. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric arsenate.
 13. A method according to claim 2 wherein said inorganic oxide gel is formed of ferric borate.
 14. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium phosphate.
 15. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium arsenate.
 16. A method according to claim 2 wherein said inorganic oxide gel is formed of chromium borate.
 17. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic hydroxide.
 18. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic borate.
 19. A method according to claim 2 wherein said inorganic oxide gel is formed of stannic tungstate.
 20. A method according to claim 1 wherein said electrolyte is sodium chloride.
 21. A method according to claim 1 wherein said electrolyte is citric acId.
 22. A method according to claim 1 wherein said electrolyte is sulfuric acid.
 23. A method according to claim 1 wherein said electrolyte is iron sulfate.
 24. A method according to claim 1 wherein said electrolyte is zinc chloride.
 25. A method according to claim 1 wherein said electrolyte is strontium90 nitrate.
 26. A method according to claim 1 wherein said electrolyte is cesium137 chloride.
 27. A method according to claim 1 wherein said electrolyte is a member selected from the group consisting of sodium, ammonium and magnesium sulfites.
 28. A method for simultaneously removing and concentrating electrolytes from aqueous solutions containing the same which comprises subjecting an aqueous electrolyte solution to contact with an unit comprising an inorganic oxide gel core encased between two membranes under the influence of an applied electrical field, allowing the electrolyte to be sorbed by said gel until saturation of said electrolyte occurs in said gel, whereby said electrolyte is resultingly exuded by said gel, and thence recovering the resultant electrolyte exudate as overflow from said gel. 